Atlas FDA

CREATINE KINASE METHOD

FDA 510(k) clearance K941584 · decided 1994-07-06

Clearance details

K-number
K941584
Device name
CREATINE KINASE METHOD
Applicant
Dupont Medical Products
Decision
Substantially Equivalent
Date received
1994-04-01
Decision date
1994-07-06
Days to decision
96 days
Clearance type
Traditional
Product code
JHS
Device class
2
Regulation number
862.1215
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Wilmington, DE, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Creatine Kinase (K160570)Roche Diagnostics Operations (Rdo)2016-05-25
CKMB UDR ASSAY (K102706)SENTINEL CH. SpA2011-08-19
S40 CREATINE KINASE (CK) (K082226)Alfa Wassermann Diagnostic Technologies, Inc.2008-09-18
THE DIMENSION VISTA FLEX REAGENT CARTRIDGES / KIT ASSAYS (K062128)Dade Behring, Inc.2006-08-21
CARESIDE CK (K990439)Careside, Inc.1999-04-19
CARESIDE CKMB (K990434)Careside, Inc.1999-04-19
IMMULITE CK-MB, CATALOG # LKCP1 (100 TESTS), LKCP5 (500 TESTS) (K981495)Diagnostic Products Corp.1998-06-10
ACS CKMB II IMMUNOASSAY (K962126)Ciba Corning Diagnostics Corp.1996-06-21
STRATUS CK-MB DENDRIMER FLUOROMETRIC ENZYME IMMUNOASSAY & STRATUS CK-MB DENDRIMER HIGH SAMPLE DILUENT (K952250)Dade Intl., Inc.1995-07-17
ACCESS CK-MB REAGENTS (K945083)Bio-Rad Laboratories, Inc.1994-11-21
KINASE ISOENZYME (K943024)Dupont Medical Products1994-08-02
ROCHE ISOMUNE- CK (K903025)Roche Diagnostic Systems, Inc.1990-08-09

Recalls involving this device

No recalls on record reference this clearance.